EP3102585B1 - Boronsäureester und pharmazeutische formulierungen daraus - Google Patents

Boronsäureester und pharmazeutische formulierungen daraus Download PDF

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EP3102585B1
EP3102585B1 EP15742988.7A EP15742988A EP3102585B1 EP 3102585 B1 EP3102585 B1 EP 3102585B1 EP 15742988 A EP15742988 A EP 15742988A EP 3102585 B1 EP3102585 B1 EP 3102585B1
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group
compound
btz
moiety
formulation
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EP3102585A1 (de
EP3102585A4 (de
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Michael Caligiuri
Robert Lee
Guido Marcucci
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Ohio State Innovation Foundation
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02—Boron compounds
    • C07F5/04—Esters of boric acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
    • A61K38/05—Dipeptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/543—Lipids, e.g. triglycerides; Polyamines, e.g. spermine or spermidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
    • A61K47/543—Lipids, e.g. triglycerides; Polyamines, e.g. spermine or spermidine
    • A61K47/544—Phospholipids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/127—Liposomes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia

Definitions

  • Boronic acid compounds display a variety of pharmaceutically useful biological activities. Shenvi et al., U.S. Pat. No. 4,499,082 discloses that peptide boronic acids are inhibitors of certain proteolytic enzymes. Kettner and Shenvi, U.S. Pat. No. 5,187,157 ; U.S. Pat. No. 5,242,904 ; and U.S. Pat. No. 5,250,720 , disclose a class of peptide boronic acids that inhibit trypsin-like proteases. Kleeman et al., U.S. Pat. No. 5,169,841 , discloses N-terminally modified peptide boronic acids that inhibit the action of renin. Kinder et al., U.S. Pat. No. 5,106,948 , discloses that certain tripeptide boronic acid compounds inhibit the growth of cancer cells.
  • the references also describe the use of boronic ester and acid compounds to reduce the rate of muscle protein degradation, to reduce the activity of NF- ⁇ B in a cell, to reduce the rate of degradation of p53 protein in a cell, to inhibit cyclin degradation in a cell, to inhibit the growth of a cancer cell, to inhibit antigen presentation in a cell, to inhibit NF- ⁇ B dependent cell adhesion, and to inhibit HIV replication.
  • Brand et al., WO 98/35691 discloses that proteasome inhibitors, including boronic acid compounds, are useful for treating infarcts such as those that occur during stroke or myocardial infarction.
  • Elliott et al., WO 99/15183 discloses that proteasome inhibitors are useful for treating inflammatory and autoimmune diseases
  • WO 02/059131 discloses compositions comprising a boronic acid compound in a lyophilized powder.
  • BTZ Bortezomib
  • BTZ is a boronic acid proteasome inhibitor currently approved by the U.S. Food and Drug Administration for the treatment of multiple myeloma and mantle cell lymphoma.
  • BTZ is administered clinically by either subcutaneous or intravenous injection. While treatment with BTZ can be effective, administration of free BTZ is plagued by high toxicity, non-specific tissue uptake, side effects, and rapid clearance from circulation. BTZ also possesses limited stability (e.g., a limited shelf life), complicating the therapeutic use of BTZ. Efforts have been made to develop improved BTZ formulations that address these shortcomings.
  • Liposomes are spherical vesicles made of a lipid bilayer (e.g ., a phospholipid bilayer) that are capable of encapsulating hydrophilic drugs in their aqueous core or hydrophobic drugs within their lipid bilayer.
  • Liposomal drugs can provide prolonged systemic circulation time, decreased drug toxicity, and enhanced drug delivery efficacy.
  • liposomal formulations of certain chemotherapeutics including daunorubicin (sold under the name DAUNOXOME by Gilead Sciences), doxorubicin (sold under the name DOXIL by Ortho Biotech and under the name CAELYX by Schering-Plough), and vincristine (sold under the name MARQIBO by Spectrum Pharmaceuticals), have been approved by the FDA and exhibit prolonged systemic circulation time, decreased drug toxicity, and enhanced drug delivery efficacy relative to alternative formulations of these chemotherapeutics.
  • daunorubicin sold under the name DAUNOXOME by Gilead Sciences
  • doxorubicin sold under the name DOXIL by Ortho Biotech and under the name CAELYX by Schering-Plough
  • vincristine sold under the name MARQIBO by Spectrum Pharmaceuticals
  • compositions and methods disclosed herein address these and other needs.
  • this disclosure in one aspect, relates to compositions and methods of making and using the compositions.
  • the subject matter disclosed herein relates to boronic acid esters of boronic acid therapeutic agents.
  • the boronic acid esters can be used to prepare liposomal formulations that contain and/or release boronic acid therapeutic agents with improved properties, such as enhanced stability.
  • the invention provides compounds according to claim 1 to 15.
  • P 1 can be an amino-group protecting moiety.
  • P 1 can be R 5 -C(O)-, R 5 -S(O) 2 -, R 5 -NH-C(O)-, or R 5 -O-C(O)-, where R 5 is an alkyl group, an aryl group, an alkylaryl group, an arylalkyl group, a cycloalkyl group, an alkylcycloalkyl group, a heterocyclyl group, an alkylheterocyclyl group, a heteroaryl group, or an alkylheteroaryl group.
  • P 1 can be R 5 -C(O)-, R 5 -S(O) 2 -, R 5 -NH-C(O)-, or R 5 -O-C(O)-, and R 5 is a heteroaryl group.
  • P 1 can be (2-pyrazine)carbonyl.
  • R 3 is an isobutyl group.
  • A comprises a lipid moiety chosen from a fatty acid, a glycerolipid, a phospholipid, a sphingolipid, a sterol, or a prenol.
  • the polyol comprises a sugar (e.g. , a monosaccharide such as fructose).
  • the polyol can comprise a reduced sugar (e.g ., a sugar alcohol such as mannitol, sorbitol, or galactitol).
  • the polyol can comprise an amino sugar (e.g., meglumine or glucamine).
  • the polyol can be meglumine, glucamine, mannitol, sorbitol, or fructose.
  • A can be a C 8 -C 40 alkyl group, a C 8 -C 40 alkenyl group, a C 8 -C 40 alkoxy group, a C 8 -C 40 alkylthio group, a C 8 -C 40 alkylsulfinyl group, a C 8 -C 40 alkylsulfonyl group, a C 8 -C 40 alkylamino group, a C 8 -C 40 dialkylamino group, a C 8 -C 40 alkylcarbon group, a C 8 -C 40 alkoxycarbonyl group, a C 8 -C 40 alkylaminocarbonyl group, a C 8 -C 40 dialkylaminocarbonyl group, or a moiety defined by the formula wherein
  • R 12 can be hydrogen.
  • R 12 is an alkyl group.
  • R 12 can be a C 1 -C 6 alkyl group.
  • R 12 can be a C 1 -C 4 alkyl group.
  • R 12 can be methyl or ethyl.
  • X can be -O-. In this disclosure, X can be -NH- or -N(CH 3 )-.
  • the compound is defined by Formula IIA wherein
  • the compound can be one of the following.
  • the boronic esters described herein can be anionic.
  • an additional deprotonated hydroxyl group can be attached to the boron atom of the compounds described herein, and the compounds can exist in a salt form.
  • compositions that include liposomes formed from a vesicle-forming lipid, and a compound described herein entrapped in the liposomes.
  • the formulation can be lyophilized.
  • the liposomal formulations can maintain stability during lyophilization, and once lyophilized, can remain stable when stored at room temperature for periods of up to six months.
  • the formulation can further include a lyoprotectant, such as sucrose or trehalose.
  • Methods can include administering to the subject a therapeutically effective amount of a compound or formulation described herein.
  • a “subject” is meant an individual.
  • the "subject” can include domesticated animals (e.g., cats, dogs, etc.), livestock (e.g., cattle, horses, pigs, sheep, goats, etc.), laboratory animals (e.g., mouse, rabbit, rat, guinea pig, etc.), and birds.
  • “Subject” can also include a mammal, such as a primate or a human.
  • reduce or other forms of the word, such as “reducing” or “reduction,” is meant lowering of an event or characteristic (e.g., tumor growth). It is understood that this is typically in relation to some standard or expected value, in other words it is relative, but that it is not always necessary for the standard or relative value to be referred to. For example, “reduces tumor growth” means reducing the rate of growth of a tumor relative to a standard or a control.
  • prevent or other forms of the word, such as “preventing” or “prevention,” is meant to stop a particular event or characteristic, to stabilize or delay the development or progression of a particular event or characteristic, or to minimize the chances that a particular event or characteristic will occur. Prevent does not require comparison to a control as it is typically more absolute than, for example, reduce. As used herein, something could be reduced but not prevented, but something that is reduced could also be prevented. Likewise, something could be prevented but not reduced, but something that is prevented could also be reduced. It is understood that where reduce or prevent are used, unless specifically indicated otherwise, the use of the other word is also expressly disclosed.
  • treat or other forms of the word, such as “treated” or “treatment,” is meant to administer a composition or to perform a method in order to reduce, prevent, inhibit, or eliminate a particular characteristic or event (e.g., tumor growth or survival).
  • control is used synonymously with the term “treat.”
  • anticancer refers to the ability to treat or control cellular proliferation and/or tumor growth at any concentration.
  • alkyl refers to saturated straight, branched, primary, secondary or tertiary hydrocarbons, including those having 1 to 20 atoms.
  • alkyl groups will include C 1 -C 12 , C 1 -C 10 , C 1 -C 8 , C 1 -C 6 , C 1 -C 5 , C 1 -C 4 , C 1 -C 8 , or C 1 -C 2 alkyl groups.
  • C 1 -C 10 alkyl groups include, but are not limited to, methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,
  • C 1 -C 4 -alkyl groups include, for example, methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, and 1,1-dimethylethyl groups.
  • Cyclic alkyl groups or "cycloalkyl” groups include cycloalkyl groups having from 3 to 10 carbon atoms. Cycloalkyl groups can include a single ring, or multiple condensed rings. In some examples, cycloalkyl groups include C 3 -C 4 , C 4 -C 7 , C 5 -C 7 , C 4 -C 6 , or C 5 -C 6 cyclic alkyl groups. Non-limiting examples of cycloalkyl groups include adamantyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and the like.
  • Alkyl and cycloalkyl groups can be unsubstituted or substituted with one or more moieties chosen from alkyl, halo, haloalkyl, hydroxyl, carboxyl, acyl, acyloxy, amino, alkyl- or dialkylamino, amido, arylamino, alkoxy, aryloxy, nitro, cyano, azido, thiol, imino, sulfonic acid, sulfate, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, phosphonyl, phosphinyl, phosphoryl, phosphine, thioester, thioether, acid halide, anhydride, oxime, hydrazine, carbamate, phosphoric acid, phosphate, phosphonate, or any other viable functional group that does not inhibit the biological activity of the compounds of the invention, either un
  • alkyl such as “alkylamino” or “dialkylamino,” will be understood to comprise an alkyl group as defined above linked to another functional group, where the group is linked to the compound through the last group listed, as understood by those of skill in the art.
  • alkenyl refers to both straight and branched carbon chains which have at least one carbon-carbon double bond.
  • alkenyl groups can include C 2 -C 20 alkenyl groups.
  • alkenyl can include C 2 -C 12 , C 2 -C 10 , C 2 -C 8 , C 2 -C 6 , or C 2 -C 4 alkenyl groups.
  • the number of double bonds is 1-3, in another embodiment of alkenyl, the number of double bonds is one or two. Other ranges of carbon-carbon double bonds and carbon numbers are also contemplated depending on the location of the alkenyl moiety on the molecule.
  • C 2 -C 10 -alkenyl groups can include more than one double bond in the chain.
  • the one or more unsaturations within the alkenyl group can be located at any position(s) within the carbon chain as valence permits.
  • the carbon atom(s) in the alkenyl group that are covalently bound to the one or more additional moieties are not part of a carbon-carbon double bond within the alkenyl group.
  • alkenyl groups include, but are not limited to, ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl; 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl
  • alkynyl refers to both straight and branched carbon chains which have at least one carbon-carbon triple bond.
  • the number of triple bonds is 1-3; in another embodiment of alkynyl, the number of triple bonds is one or two.
  • alkynyl groups include from C 2 -C 20 alkynyl groups.
  • alkynyl groups can include C 2 -C 12 , C 2 -C 10 , C 2 -C 8 , C 2 -C 6 or C 2 -C 4 alkynyl groups.
  • Other ranges of carbon-carbon triple bonds and carbon numbers are also contemplated depending on the location of the alkenyl moiety on the molecule.
  • C 2 -C 10 -alkynyl refers to a straight-chain or branched unsaturated hydrocarbon group having 2 to 10 carbon atoms and containing at least one triple bond, such as ethynyl, prop-1-yn-1-yl, prop-2-yn-1-yl, n-but-1-yn-1-yl, n-but-1-yn-3-yl, n-but-1-yn4-yl, n-but-2-yn-1-yl, n-pent-1-yn-1-yl, n-pent-1-yn-3-yl, n-pent-1-yn-4-yl, n-pent-1-yn-5-yl, n-pent-2-yn-1-yl, n-pent-2-yn-4-yl, n-pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl, 3-methylbut-1-yn-3-yl, 3-methyl
  • Alkenyl and alkynyl groups can be unsubstituted or substituted with one or more moieties chosen from alkyl, halo, haloalkyl, hydroxyl, carboxyl, acyl, acyloxy, amino, alkyl- or dialkylamino, amido, arylamino, alkoxy, aryloxy, nitro, cyano, azido, thiol, imino, sulfonic acid, sulfate, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, phosphonyl, phosphinyl, phosphoryl, phosphine, thioester, thioether, acid halide, anhydride, oxime, hydrazine, carbamate, phosphoric acid, phosphate, phosphonate, or any other viable functional group that does not inhibit the biological activity of the compounds of the invention, either un
  • aryl refers to a monovalent aromatic carbocyclic group of from 6 to 14 carbon atoms.
  • Aryl groups can include a single ring or multiple condensed rings. In some examples, aryl groups include C 6 -C 10 aryl groups.
  • Aryl groups include, but are not limited to, phenyl, biphenyl, naphthyl, tetrahydronaphtyl, phenylcyclopropyl and indanyl.
  • Aryl groups can be unsubstituted or substituted by one or more moieties chosen from halo, cyano, nitro, hydroxy, mercapto, amino, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, haloalkyl, haloalkenyl, haloalkynyl, halocycloalkyl, halocycloalkenyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, haloalkenyloxy, haloalkynyloxy, cycloalkoxy, cycloalkenyloxy, halocycloalkoxy, halocycloalkenyloxy, alkylthio, haloalkylthio, cycloalkylthio, halocycloalkylthio, alkylsulfinyl, alkenylsulfinyl, alky
  • alkylaryl refers to an aryl group that is bonded to a parent compound through a diradical alkylene bridge, (-CH 2 -) n , where n is 1-12 (e.g., n is from 1 to 6) and where "aryl” is as defined above.
  • arylalkyl refers to an aryl group, as defined above, which is substituted by an alkyl group, as defined above.
  • alkylcycloalkyl refers to a cycloalkyl group that is bonded to a parent compound through a diradical alkylene bridge, (-CH 2 -) n , where n is 1-12 ( e.g., n is from 1 to 6) and where "cycloalkyl" is as defined above.
  • alkoxy refers to alkyl-O-, wherein alkyl refers to an alkyl group, as defined above.
  • alkenyloxy refers to the groups alkenyl-O-, alkynyl-O-, and cycloalkyl-O-, respectively, wherein alkenyl, alkynyl, and cycloalkyl are as defined above.
  • C 1 -C 6 -alkoxy groups include, but are not limited to, methoxy, ethoxy, C 2 H 5 -CH 2 O-, (CH 3 ) 2 CHO-, n-butoxy, C 2 H 5 -CH(CH 3 )O-, (CH 3 ) 2 CH-CH 2 O-, (CH 3 ) 3 CO-, n-pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, n-hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylprop
  • alkylthio refers to alkyl-S-, wherein alkyl refers to an alkyl group, as defined above.
  • cycloalkylthio refers to cycloalkyl-S-where cycloalkyl are as defined above.
  • alkylsulfinyl refers to alkyl-S(O)-, wherein alkyl refers to an alkyl group, as defined above.
  • alkylsulfonyl refers to alkyl-S(O) 2 -, wherein alkyl is as defined above.
  • alkylamino and “dialkylamino,” as used herein, refer to alkyl-NH- and (alkyl)2N- groups, where alkyl is as defined above.
  • alkylcarbonyl refers to alkyl-C(O)-, alkoxy-C(O)-, alkylamino-C(O)- and dialkylamino-C(O)- respectively, where alkyl, alkoxy, alkylamino, and dialkylamino are as defined above.
  • heteroaryl refers to a monovalent aromatic group of from 1 to 15 carbon atoms ( e.g., from 1 to 10 carbon atoms, from 2 to 8 carbon atoms, from 3 to 6 carbon atoms, or from 4 to 6 carbon atoms) having one or more heteroatoms within the ring.
  • the heteroaryl group can include from 1 to 4 heteroatoms, from 1 to 3 heteroatoms, or from 1 to 2 heteroatoms.
  • the heteroatom(s) incorporated into the ring are oxygen, nitrogen, sulfur, or combinations thereof. When present, the nitrogen and sulfur heteroatoms can optionally be oxidized.
  • Heteroaryl groups can have a single ring ( e.g., pyridyl or furyl) or multiple condensed rings provided that the point of attachment is through a heteroaryl ring atom.
  • Preferred heteroaryls include pyridyl, piridazinyl, pyrimidinyl, pyrazinyl, triazinyl, pyrrolyl, indolyl, quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinnyl, furanyl, thiophenyl, furyl, pyrrolyl, imidazolyl, oxazolyl, isoxazolyl, isothiazolyl, pyrazolyl benzofuranyl, and benzothiophenyl.
  • Heteroaryl rings can be unsubstituted or substituted by one or more moieties as described for aryl above.
  • alkylheteroaryl refers to a heteroaryl group that is bonded to a parent compound through a diradical alkylene bridge, (-CH 2 -) n , where n is 1-12 and where "heteroaryl" is as defined above.
  • heterocyclyl refers to fully saturated or unsaturated, cyclic groups, for example, 3 to 7 membered monocyclic or 4 to 7 membered monocyclic; 7 to 11 membered bicyclic, or 10 to 15 membered tricyclic ring systems, having one or more heteroatoms within the ring.
  • the heterocyclyl group can include from 1 to 4 heteroatoms, from 1 to 3 heteroatoms, or from 1 to 2 heteroatoms.
  • the heteroatom(s) incorporated into the ring are oxygen, nitrogen, sulfur, or combinations thereof.
  • the nitrogen and sulfur heteroatoms can optionally be oxidized, and the nitrogen heteroatoms can optionally be quaternized.
  • the heterocyclyl group can be attached at any heteroatom or carbon atom of the ring or ring system and can be unsubstituted or substituted by one or more moieties as described for aryl groups above.
  • Exemplary monocyclic heterocyclic groups include, but are not limited to, pyrrolidinyl, pyrrolyl, pyrazolyl, oxetanyl, pyrazolinyl, imidazolyl, imidazolinyl, imidazolidinyl, oxazolyl, oxazolidinyl, isoxazolinyl, isoxazolyl, thiazolyl, thiadiazolyl, thiazolidinyl, isothiazolyl, isothiazolidinyl, furyl, tetrahydrofuryl, thienyl, oxadiazolyl, piperidinyl, piperazinyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolodinyl, 2-oxoazcpinyl, azcpinyl, 4-pipcridonyl, pyridinyl, pyrazinyl,
  • bicyclic heterocyclic groups include, but are not limited to, indolyl, benzothiazolyl, benzoxazolyl, benzodioxolyl, benzothienyl, quinuclidinyl, quinolinyl, tetra-hydroisoquinolinyl, isoquinolinyl, benzimidazolyl, benzopyranyl, indolizinyl, benzofuryl, chromonyl, coumarinyl, benzopyranyl, cinnolinyl, quinoxalinyl, indazolyl, pyrrolopyridyl, furopyridinyl (such as furo[2,3-c]pyridinyl, furo[3,2-b]pyridinyl]or furo[2,3-b]pyridinyl), dihydroisoindolyl, dihydroquinazolinyl (such as 3,4-dihydro-4-oxo-
  • Exemplary tricyclic heterocyclic groups include carbazolyl, benzidolyl, phenanthrolinyl, acridinyl, phenanthridinyl, xanthenyl, and the like.
  • alkylheterocyclyl refers to a heterocyclyl group that is bonded to a parent compound through a diradical alkylene bridge, (-CH 2 -) n , where n is 1-12 and where "heterocyclyl” is as defined above.
  • heterocyclylalkyl refers to a heterocyclyl group, as defined above, which is substituted by an alkyl group, as defined above.
  • Heretrocyclyl and heteroaryl groups can be unsubstituted or substituted with one or more moieties chosen from alkyl, halo, haloalkyl, hydroxyl, carboxyl, acyl, acyloxy, amino, alkyl- or dialkylamino, amido, arylamino, alkoxy, aryloxy, nitro, cyano, azido, thiol, imino, sulfonic acid, sulfate, sulfonyl, sulfanyl, sulfinyl, sulfamonyl, ester, phosphonyl, phosphinyl, phosphoryl, phosphine, thioester, thioether, acid halide, anhydride, oxime, hydrazine, carbamate, phosphoric acid, phosphate, phosphonate, or any other viable functional group that does not inhibit the biological activity of the compounds of the invention, either unprotect
  • halogen refers to the atoms fluorine, chlorine, bromine and iodine.
  • halo- e.g., as illustrated by the term haloalkyl
  • haloalkyl refers to all degrees of halogen substitution, from a single substitution to a perhalo substitution ( e.g., as illustrated with methyl as chloromethyl (-CH 2 Cl), dichloromethyl (-CHCl 2 ), trichloromethyl (-CCl 3 )).
  • the term "substituted" is contemplated to include all permissible substituents of organic compounds.
  • the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, and aromatic and nonaromatic substituents of organic compounds.
  • Illustrative substituents include, for example, those described below.
  • the permissible substituents can be one or more and the same or different for appropriate organic compounds.
  • the heteroatoms, such as nitrogen can have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valences of the heteroatoms.
  • substitution or “substituted with” include the implicit proviso that such substitution is in accordance with permitted valence of the substituted atom and the substituent, and that the substitution results in a stable compound, e.g., a compound that does not spontaneously undergo transformation such as by rearrangement, cyclization, elimination, etc.
  • a formula with chemical bonds shown only as solid lines and not as wedges or dashed lines contemplates each possible isomer, e.g., each enantiomer, diastereomer, and meso compound, and a mixture of isomers, such as a racemic or scalemic mixture.
  • boronic acid esters of boronic acid therapeutic agents can function as prodrugs for the boronic acid therapeutic agents.
  • the boronic acid esters can be used to prepare liposomal formulations with improved properties, such as enhanced stability.
  • P 1 is an amino-group protecting moiety.
  • Amino-group protecting moieties include groups that are used to derivatize an amino group, especially an N-terminal amino group of a peptide or amino acid. Such groups include, without limitation, alkyl, acyl, alkoxycarbonyl, aminocarbonyl, and sulfonyl moieties.
  • amino-group protecting moiety is not intended to be limited to those particular protecting groups that are commonly employed in organic synthesis, nor is it intended to be limited to groups that are readily cleavable.
  • P 1 is R 5 -C(O)-, R 5 -S(O) 2 -, R 5 -NH-C(O)-, or R 5 -O-C(O)-, wherein R 5 is an alkyl group, an aryl group, an alkylaryl group, an arylalkyl group, a cycloalkyl group, an alkylcycloalkyl group, a heterocyclyl group, an alkylheterocyclyl group, a heteroaryl group, or an alkylheteroaryl group.
  • P 1 is R 5 -C(O)-, R 5 -S(O) 2 -, R 5 -NH-C(O)-, or R 5 -O-C(O)-, and R 5 is a heteroaryl group.
  • P 1 is (2-pyrazine)carbonyl.
  • R 0 is hydrogen.
  • R 0 is an alkyl group.
  • R 0 can be a C 1 -C 6 alkyl group.
  • R 0 can be a C 1 -C 4 alkyl group.
  • R 0 can be methyl or ethyl.
  • R 1 , R 2 , and R 3 are each independently chosen from hydrogen, C 1 -Cs alkyl, C 3 -C 10 cycloalkyl, C 6 -C 10 aryl, and -CH 2 -R 4 , wherein each of R 1 , R 2 , R 3 , and R 4 can be optionally substituted as described above.
  • R 1 , R 2 , and R 3 are each independently chosen from C 1 -C 4 alkyl and -CH 2 -R 4 , and R 4 is one of cycloalkyl, aryl, heterocyclyl, heteroaryl, or alkoxy.
  • R 1 , R 2 , and R 3 are each independently chosen from C 1 -C 4 alkyl and -CH 2 -R 4 , and R 4 is one of C 6 -C 10 aryl, (C 6 -C 10 )ar(C 1 -C 6 )alkyl, (C 1 -C 6 )alk(C 6 -C 10 )aryl, C 3 -C 10 cycloalkyl, C 1 -C 8 alkoxy, or C 1 -C 8 , alkylthio or a 5- to 10-membered heteroaryl ring.
  • R 3 is an isobutyl group.
  • m can be 0, 1, or 2.
  • the boronate ester compound is a dipeptide.
  • the residue within the brackets is present, and the compound is a tripeptide.
  • the compound is a tetrapeptide.
  • m is zero.
  • the terms "peptide,” 'dipeptide,” and “tripeptide,” as used here, are intended to encompass compounds comprising natural amino acid residues, unnatural amino acid residues, or a combination of natural and unnatural amino acid residues. It will be apparent that the terms "peptide,” “dipeptide,” and “tripeptide” are used to refer to compounds herein in which the carboxylic acid functionality of the C-terminal amino acid residue is replaced by a boronate ester functionality.
  • the term "moiety derived from a polyol” refers to a moiety formed by removing the hydrogen atoms from two hydroxyl groups of a polyol ( i.e., a moiety that includes two or more hydroxyl groups).
  • the polyol can include any number of hydroxyl groups.
  • the polyol can include from 2 to 8 hydroxyl groups ( e.g., from 2 to 6 hydroxyl groups).
  • the polyol can include at least 3 hydroxyl groups ( e.g., from 3 to 8 hydroxyl groups, from 3 to 6 hydroxyl groups, or from 3 to 5 hydroxyl groups).
  • the moiety derived from a polyol can be attached to the boron atom by any two hydroxyl groups of the polyol, such that the resulting boronate ester forms 5-, 6-, 7-, 8-, or 9-membered ring. In some examples, the boronate ester forms a 5- or 6-membered ring.
  • the polyol can include a 1,2-diol or 1,3-diol functionality.
  • the polyol can be any suitable polyol.
  • the polyol can be a polymeric polyol (e.g., polyvinyl alcohol), an aromatic polyol (e.g., a catechol or catechol derivative), or a sugar (e.g., a monosaccharide, a disaccharide, an oligosaccharide, or a polysaccharide).
  • the polyol can be a non-aromatic polyol (i.e., the polyol does not include an aromatic moiety).
  • the polyol comprises a sugar (e.g., a monosaccharide such as fructose).
  • the polyol can comprise a reduced sugar (e.g., a sugar alcohol such as mannitol, sorbitol, or galactitol).
  • the polyol can comprise an amino sugar (e.g., meglumine or glucamine).
  • the polyol is meglumine, glucamine, mannitol, sorbitol, or fructose.
  • L is absent (i.e., Z is directly bound to A).
  • Z is directly bound to A.
  • L is present, and is a linking group.
  • the linking group can be, for example, an alkylene, heteroalkylene, alkenylene, heteroalkenylene, alkynylene, heteroalkynylene, cycloalkylene, alkylcycloalkylene, cycloalkylalkylene, heterocyclylene, alkylheterocyclylene, heterocyclylalkylene, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, heteroalkylaminocarbonyl, dialkylaminocarbonyl, or heterodialkylaminocarbonyl group through which Z is bound to A.
  • such linking groups can further include one or more functional groups, such as the linking moieties described below.
  • the linking group can also be a linking moiety that links Z to A.
  • Suitable linking moieties are known in the art, and include, for example, secondary amides (-CONH-), tertiary amides (-CONR-), secondary carbamates (-OCONH-; -NHCOO-), tertiary carbamates (-OCONR-; -NRCOO-), ureas (-NHCONH-; -NRCONH-; -NHCONR-, -NRCONR-), carbinols (-CHOH-, -CROH-), ethers (-O-), and esters (-COO-, -CH 2 O 2 C-, CHRO 2 C-), imines, and disulfide linkages, wherein R is an alkyl group, an aryl group, or a heterocyclyl group.
  • A can be any suitable lipophilic moiety.
  • the lipophilic moiety can comprise a moiety derived from a lipid (e.g., a moiety formed by covalent reaction of a lipid with Z or L, when present).
  • the lipid can be any suitable naturally occurring or synthetic lipid.
  • the lipid can comprise a fatty acid, a glycerolipid, a phospholipid, a sphingolipid, a sterol, or a prenol.
  • the lipid can comprise a fatty acid.
  • Fatty acids include a hydrocarbon chain that terminates with a carboxylic acid group.
  • the fatty acid can include at least 12 carbon atoms.
  • the fatty acid can be a saturated, monounsaturated or polyunsaturated fatty acid.
  • the fatty acid can be a fatty acid that is naturally occurring in humans.
  • Suitable fatty acids include myristic (12:0, tetradecanoic), palmitic (16:0, hexadecanoic), stearic (18:0, octadecanoic), arachidic (20:0, eicosanoic), and behenic (22:0, docosanoic) saturated fatty acids; palmitoleic (16:1(n-7), cis-9-hexadecenoic), petroselinic (18:1(n-12), cis-6-octadecenoic), oleic (18:1(n-9), cis-octadecenoic, cis-vaccenic (18:1(n-7), cis-11-octadecenoic), erucic (22:1(n-9), cis-13-docosenoic monounsaturated fatty acids; and linoleic (18:2(n)
  • Fatty acid derivatives with substituents or branching along the carbon chain can also be used in the present invention provided that the lipid character of the derivatized fatty acid is maintained.
  • the fatty acid can be a branched chain fatty acid possessing from 10 to 30 carbon atoms. Branches can include one or more methyl groups substituted at any position along the saturated or unsaturated fatty acid chain, or involve larger alkyl groups.
  • Other useful fatty acids include those with one or more alicyclic rings along the fatty acid backbone or at a terminal position. Further useful fatty acids also include hydroxy fatty acids, wherein the hydroxy group is within two carbons of the carboxylic acid (a- and ⁇ -hydroxy fatty acids).
  • the ⁇ - or ⁇ -hydroxy group of the hydroxy fatty acids can also be further derivatized through the formation of ethers or ester to add a second fatty acid chain to the lipid, thereby increasing its lipophilic character.
  • fatty acids also applies to their use in the following types of lipids where the lipids contain fatty acid components.
  • the above fatty acids can be modified to better facilitate covalent or noncovalent binding to Z or L by, for example, converting the acid head group to an alcohol or amine, an alcohol further derivatized as a leaving group, or a leaving group.
  • the fatty acid can be derivatized by adding a short spacer, e.g., formation of esters with 2-aminoethanol, ethylene glycol or other ethanol derivatives possessing a desired functional group. All chemistry required to prepare such modified fatty acids are believed to be routine and known by chemists skilled in organic synthesis.
  • the lipid can comprise a fatty amide.
  • Fatty amides are amide analogues of fatty acids. Suitable fatty amides include those in which a fatty acid, as described above, is converted to an amide by, for example, treatment with 2-aminoethanol, thus providing an alcohol that can be further modified, if desired.
  • fatty amides can be formed using diamines, such as 1,2-diaminoethane, thus providing a primary amine for facilitating linkage to Z or L.
  • Suitable fatty amides can also be formed using fatty acids and amino acids, which can then be further derivatized, if desired.
  • Example fatty amides include anandamide, N-arachidonoylglycine, and N-palmitoylethanolamide.
  • the lipid can comprise a glycerolipid.
  • Suitable glycerolipids include mono- and diacylglycerolipids (e.g., mono- and diacylglycerols and glycosylglycerols) that include fatty acids, as described above.
  • the lipid can comprise a phospholipid.
  • suitable phospholipids include phosphatidylethanolamines (cephalins), phosphatidylcholines, phosphatidylserines, phosphatidyl-L-threonines, phosphatidylglycerols, phosphatidylinositols, phosphatidic acids, bisphosphatidyl glycerols (cardiolipins), and phosphoglycolipids.
  • Suitable phospholipids include ether phospholipids (e.g., alkylacyl phospholipids and alkenylacyl phospholipids), lysophospholipids, and any of the above phospholipids in which one of the fatty acid chains has be hydrolyzed to give a monoacyl, monoalkyl or monoalkenylphospholipid.
  • the lipid can comprise a sphingolipid.
  • suitable sphingolipids include sphingosine and other sphingoid bases, ceramides, ceramide phospholipids, and glycosphingolipids.
  • ceramide phospholipids include sphingolipids other than sphingomyelin in which a ceramide is bound to a phosphate group ( e.g ., sphingolipids such as ceramide phosphorylethanolamines, ceramide phosphorylglycerols, and ceramide inositols).
  • Suitable sphingoid bases can include analogues of sphingoid bases with differing carbon chains (length, unsaturation, hydroxylation).
  • the carbon chains in the sphingoid base can include from 14-24 carbon atoms.
  • Suitable sphingoid bases include sphingosine (d18:1, d18:1 ⁇ 4t , 4E-d18:1, or its cis isomer: d18:1 ⁇ 4c , 4Z-d18:1) dihydrosphingosine (d18:0, sphinganine), phytosphingosine (t18:0), and dehydrophytosphingosine (t18:1, t18:1 ⁇ 8t , 8E-t18:1, or is cis isomer: t18:1 ⁇ 8c , 8Z-t18:1), and eicosasphingosine (d20:1, 4E-d20:1, d20:1 ⁇ 4t ).
  • the lipid can comprise a sterol.
  • Suitable sterol lipids include sterols, and oxysterols in which the A or B ring of the cholesterol is oxidized rather than the alkyl chain, such as 7 ⁇ -hydroxycholesterol or 4 ⁇ -hydroxycholesterol.
  • Other suitable oxysterols include oxysterols in which the alkyl side chain of the cholesterol has been hydroxylated (and optionally converted to an amine) and the A and B rings of the cholesterol skeleton are in a reduced form ( i.e., dehydroxylated).
  • Other suitable oxysterols include oxysterols possessing a primary hydroxy group that is oxidized to a carboxylic acid, including examples where the carboxylic acid has been esterified (e.g., with 2-aminoethanol).
  • suitable sterols can include sterols from other origins, such as plant-based sterols (phytosterols).
  • phytosterols include, but are not limited to, campesterol, sitosterol, brassicasterol, stigmasterol, avenasterol.
  • Suitable sterols include derivatized sterols.
  • Sterols can also be derivatized by adding, for example, 2-aminoethanol, inositol, serine, glycoside, phosphorylethanolamine, phosphonylethanolamine, phosphorylserine, phosphorylinositol, phosphorylglycosides, or glycosides derivatized with 2-aminoethanol, serine, phosphorylethanolamine, or phosphonylethanolamine, to the 3-hydroxy substituent of the A-ring or a hydroxy substituent of the alkyl side chain of any of the above sterols or oxysterols.
  • the lipid can comprise a prenol.
  • Suitable prenol lipids can include fat-soluble vitamins (e.g., vitamins A, E, and K), as well as other prenol lipids, including other tocopherols, tocotrienols, retinoic acid, dolichols, and polyprenols.
  • Other suitable prenols include diphosphate derivatives of prenols, such as famesyl pyrophosphate and presqualene diphosphate.
  • Prenol lipids can also be further derivatized by, for example, adding 2-aminoethanol, inositol, serine, glycoside, phosphorylethanolamine, phosphonylethanolamine, phosphorylserine, phosphorylinositol, phosphorylglycosides, or glycosides derivatized with 2-aminoethanol, serine, phosphorylethanolamine, or phosphonylethanolamine, to an available hydroxy substituent.
  • A is a C 8 -C 40 alkyl group, a C 8 -C 40 alkenyl group, a C 8 -C 40 alkoxy group, a C 8 -C 40 alkylthio group, a C 8 -C 40 alkylsulfinyl group, a C 8 -C 40 alkylsulfonyl group, a C 8 -C 40 alkylamino group, a C 8 -C 40 dialkylamino group, a C 8 -C 40 alkylcarbonyl group, a C 8 -C 40 alkoxycarbonyl group, a C 8 -C 40 alkylaminocarbonyl group, a C 8 -C 40 dialkylaminocarbonyl group, or a moiety defined by the formula below wherein
  • A is a moiety defined by the formula below where the dotted lines indicate that a single or double bond can be present; and R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 are as defined above. In one embodiment, A is defined by the structure below.
  • the compound can be defined by Formula IA wherein
  • A comprises a lipid moiety chosen from a fatty acid, a glycerolipid, a phospholipid, a sphingolipid, a sterol, or a prenol.
  • the compound can be defined by Formula II wherein
  • R 12 is hydrogen. In other examples, R 12 is an alkyl group.
  • R 12 can be a C 1 -C 6 alkyl group.
  • R 12 can be a C 1 -C 4 alkyl group.
  • R 12 can be methyl or ethyl.
  • X is -O-. In other examples, X is -NH- or -N(CH 3 )-.
  • the compound can be defined by Formula IIA wherein
  • the compound can be one of the following.
  • compositions including the compounds described herein.
  • Pharmaceutical formulations can include a therapeutically effective amount of a compound described herein in combination with one or more pharmaceutically acceptable excipients.
  • Representative excipients include solvents, diluents, pH modifying agents, preservatives, antioxidants, suspending agents, wetting agents, viscosity modifiers, tonicity agents, stabilizing agents, and combinations thereof.
  • Suitable pharmaceutically acceptable excipients are preferably selected from materials that are generally recognized as safe (GRAS) by the FDA, and can be administered to an individual without causing undesirable biological side effects or unwanted interactions.
  • the pharmaceutical formulation can be a liposomal formulation.
  • pharmaceutical formulations that include liposomes formed from a vesicle-forming lipid, and a compound described herein entrapped in the liposomes.
  • a compound entrapped in a liposome can be sequestered in the central aqueous compartment of the liposome, in the aqueous space between liposome lipid bilayers, or within a bilayer of the liposome itself.
  • the liposomes in the formulation can be composed primarily of vesicle-forming lipids.
  • a vesicle-forming lipid is one that can form spontaneously into bilayer vesicles in water, as exemplified by the phospholipids, with its hydrophobic moiety in contact with the interior, hydrophobic region of the bilayer membrane, and its head group moiety oriented toward the exterior, polar surface of the membrane.
  • Lipids capable of stable incorporation into lipid bilayers, such as cholesterol and its various analogs can also be used in the liposomes.
  • the vesicle-forming lipids are preferably lipids having two hydrocarbon chains, typically acyl chains, and a head group, either polar or nonpolar.
  • lipids such as phosphatidylcholine, phosphatidylethanolamine, phosphatidic acid, phosphatidylinositol, and sphingomyelin, where the two hydrocarbon chains are typically between about 14-22 carbon atoms in length, and have varying degrees of unsaturation.
  • phospholipids such as phosphatidylcholine, phosphatidylethanolamine, phosphatidic acid, phosphatidylinositol, and sphingomyelin
  • the above-described lipids and phospholipids whose acyl chains have varying degrees of saturation can be obtained commercially or prepared according to published methods.
  • suitable lipids include glycolipids, cerebrosides and sterols, such as cholesterol.
  • the vesicle-forming lipid can be selected to achieve a specified degree of fluidity or rigidity, to control the stability of the liposome in serum, and/or to control the rate of release of the entrapped agent in the liposome.
  • Liposomes having a more rigid lipid bilayer, or a gel-phase bilayer are achieved by incorporation of a relatively rigid lipid, e.g., a lipid having a relatively high phase transition temperature, e.g., up to 60° C.
  • Rigid, i.e., saturated, lipids contribute to greater membrane rigidity in the lipid bilayer.
  • Other lipid components, such as cholesterol are also known to contribute to membrane rigidity in lipid bilayer structures.
  • lipid fluidity is achieved by incorporation of a relatively fluid lipid, typically one having a lipid phase with a relatively low gel to liquid-crystalline phase transition temperature, e.g., at or below room temperature.
  • the liposomes can optionally include a vesicle-forming lipid covalently linked to a hydrophilic polymer.
  • a hydrophilic polymer As has been described, for example in U.S. Pat. No. 5,013,556 , including such a polymer-derivatized lipid in the liposome composition forms a surface coating of hydrophilic polymer chains around the liposome. The surface coating of hydrophilic polymer chains is effective to increase the in vivo blood circulation lifetime of the liposomes when compared to liposomes lacking such a coating.
  • Polymer-derivatized lipids comprised of methoxy(polyethylene glycol) (mPEG) and a phosphatidylethanolamine (e.g., dimyristoyl phosphatidylethanolamine, dipalmitoyl phosphatidylethanolamine, distearoyl phosphatidylethanolamine (DSPE), or dioleoyl phosphatidylethanolamine) can be obtained from Avanti Polar Lipids, Inc. (Alabaster, Ala.) at various mPEG molccular weights (350, 550, 750, 1,000, 2,000, 3,000, and 5,000 Daltons).
  • mPEG methoxy(polyethylene glycol)
  • a phosphatidylethanolamine e.g., dimyristoyl phosphatidylethanolamine, dipalmitoyl phosphatidylethanolamine, distearoyl phosphatidylethanolamine (DSPE), or dioleoyl phosphat
  • Lipopolymers of mPEG-ceramide can also be purchased from Avanti Polar Lipids, Inc. Preparation of lipid-polymer conjugates is also described in the literature, see U.S. Pat. Nos. 5,631,018 , 6,586,001 , and 5,013,556 ; Zalipsky, S. et al., Bioconjugate Chem. 8:111 (1997 ); Zalipsky, S. et al., Meth. Enzymol. 387:50 (2004 ). These lipopolymers can be prepared as well-defined, homogeneous materials of high purity, with minimal molecular weight dispersity ( Zalipsky, S. et al., Bioconjugate Chem.
  • the lipopolymer can also be a "neutral" lipopolymer, such as a polymer-distearoyl conjugate, as described in U.S. Pat. No. 6,586,001 .
  • lipid-polymer conjugate typically between 1-20 mole percent of the lipid-polymer conjugate is incorporated into the total lipid mixture (see, e.g., U.S. Pat. No. 5,013,556 ).
  • the liposomes can include a ligand, such as a targeting ligand, conjugated to the liposome.
  • the liposomes can optionally include a lipopolymer modified to include a ligand, forming a lipid-polymer-ligand conjugate, also referred to herein as a 'lipopolymer-ligand conjugate'.
  • the ligand can be a therapeutic molecule, such as a drug or a biological molecule having activity in vivo, a diagnostic molecule, such as a contrast agent or a biological molecule, or a targeting molecule having binding affinity for a binding partner, preferably a binding partner on the surface of a cell.
  • the ligand can have binding affinity for the surface of a cell, so as to facilitate entry of the liposome into the cytoplasm of a cell via internalization.
  • a ligand present in liposomes that include such a lipopolymer-ligand is oriented outwardly from the liposome surface, and therefore available for interaction with its cognate receptor.
  • Functionalized polymer-lipid conjugates can also be obtained commercially, such as end-functionalized PEG-lipid conjugates (Avanti Polar Lipids, Inc.).
  • the linkage between the ligand and the polymer can be a stable covalent linkage or a releasable linkage that is cleaved in response to a stimulus, such as a change in pH or presence of a reducing agent.
  • the ligand can be a molecule that has binding affinity for a cell receptor or for a pathogen circulating in the blood.
  • the ligand can also be a therapeutic or diagnostic molecule, in particular molecules that when administered in free form have a short blood circulation lifetime.
  • the ligand is a biological ligand, such as a ligand having binding affinity for a cell receptor.
  • Example biological ligands include molecules having binding affinity to receptors for CD4, folate, insulin, LDL, vitamins, transferrin, asialoglycoprotein, selectins, such as E, L, and P selectins, Flk-1,2, FGF, EGF, integrins, in particular, ⁇ 4 ⁇ 1 ⁇ v ⁇ 3 , ⁇ v ⁇ 1 ⁇ v ⁇ 5 , ⁇ v ⁇ 6 integrins, HER2, and others.
  • Ligands are known in the art, and can include proteins and peptides, including antibodies and antibody fragments, such as F(ab') 2 , F(ab) 2 , Fab', Fab, Fv (fragments consisting of the variable regions of the heavy and light chains), and scFv (recombinant single chain polypeptide molecules in which light and heavy variable regions are connected by a peptide linker), and the like.
  • the ligand can also be a small molecule peptidomimetic. It will be appreciated that a cell surface receptor, or fragment thereof, can serve as the ligand.
  • example targeting ligands include, but are not limited to vitamin molecules (e.g., biotin, folate, cyanocobalamine), oligopeptides, oligosaccharides.
  • vitamin molecules e.g., biotin, folate, cyanocobalamine
  • oligopeptides oligosaccharides.
  • Other example ligands include those described in U.S. Pat. Nos. 6,214,388 , 6,316,024 , 6,056,973 , and 6,043,094 .
  • Liposomal formulations including the compounds described herein can be formed using any suitable method for preparing and/or loading liposomes.
  • a compound described herein and one or more vesicle-forming lipids can be dissolved in a suitable solvent, and the solvent can be evaporated to form a lipid film.
  • the lipid film can be hydrated with an aqueous solution (e.g., having a pH of from 7-9) to form liposomes comprising the entrapped compound.
  • the liposomes can be sized to obtain a population of liposomes having a substantially homogeneous size range, for example from 0.01 to 0.5 microns (e.g., from 0.03-0.40 microns).
  • Liposomes can be sized by any suitable method, such as by extrusion through a series of membranes having a selected uniform pore size (e.g., polycarbonate membranes having a selected uniform pore size in the range of 0.03 to 0.2 micron).
  • the pore size of the membrane corresponds roughly to the largest sizes of liposomes produced by extrusion through that membrane, particularly where the preparation is extruded two or more times through the same membrane.
  • Homogenization methods can also be used to prepare liposomes having sizes of 100 nm or less ( Martin, F. J., in Specialized Drug Delivery Systems-Manufacturing and Production Technology, P. Tyle, Ed., Marcel Dekker, New York, pp. 267-316 (1990 )).
  • the liposomes in the formulation can have an average particle size, as measured by dynamic light scattering, of from 50 nm to 250 nm (e.g., from 50 nm to 200 nm, from 75 nm to 150 nm, from 90 nm to 150 nm, from 120 nm to 150 nm, from 100 nm to 130 nm, or from 90 nm to 110 nm).
  • an average particle size as measured by dynamic light scattering
  • the liposomes in the formulation can have a zeta potential of from -50 mV to 0 mV (e.g., from -25 mV to 0 mV, from -15 mV to 0 mV, or from -10 mV to 0 mV).
  • unencapsulated compound can be removed by a suitable technique, such as dialysis, centrifugation, tangential-flow diafiltration, size exclusion chromatography or ion exchange to achieve a suspension of liposomes having a high concentration of entrapped compound in the liposomes and little to no compound in solution outside of the liposomes.
  • a suitable technique such as dialysis, centrifugation, tangential-flow diafiltration, size exclusion chromatography or ion exchange to achieve a suspension of liposomes having a high concentration of entrapped compound in the liposomes and little to no compound in solution outside of the liposomes.
  • the external phase of the liposomes can be adjusted, if desired, by titration, dialysis or the like, to an appropriate pH.
  • the liposomal suspension can be lyophilized using methods known in the art.
  • the resulting composition can be in the form of a lyophilized powder.
  • lyophilized powder refers to any solid material obtained by lyophilization of an aqueous mixture.
  • a lyoprotectant such as sucrose or trehalose, can be added to the liposomal formulation prior lyophilization.
  • Stability of the lyophilized formulation can be assessed by visual inspection for appearance of cake, the time of reconstitution, and the property of the reconstituted liposomes after various lengths of storage time.
  • a liposomal formulation can be assessed for appearance of particulates or turbidity by visual inspection, change in color, mean particle size and polydispersity index by dynamic light scattering on a particle size analyzer (e.g., using a NICOMP370 particle sizing system), zeta potential measurement (e.g., using Malvern Instrument's Zetasizer), percentage of drug encapsulation by chromatography (e.g., by size-exclusion chromatography on a Sepharose CL-4B column), chemical integrity of the drug substance and of excipients and appearance of decomposition products by HPLC and by LC-MS.
  • the preferred stability range for the BTZ liposome formulation is less than 20% change in mean particle size and drug encapsulation percentage after 6 months storage at 4 degree compared to immediately reconstituted sample;
  • Lyophilized formulations can be readily reconstituted prior to administration by adding an aqueous solvent.
  • the reconstitution solvent can be suitable for pharmaceutical administration (e.g., for parenteral administration to a subject).
  • suitable reconstitution solvents include, without limitation, water, saline, and phosphate buffered saline (PBS).
  • the liposomal formulation described herein can be used in combination with other anticancer agents, including various chemotherapeutic agents, such as cytarabine, fludarabine, decitabine, daunorubicin, and therapeutic antibodies such as rituximab, alemtuzumab, tyrosine kinase inhibitors, and any other agents with anticancer activities.
  • anticancer agents can be co-formulated in the same liposome formulation as the boronic acid agent.
  • daunorubicin or cytarabine can be co-encapsulated into liposomal bortezomib at a defined drug ratio.
  • Such type of combination can mediate co-delivery of the therapeutic combination at a ratio that produces optimal therapeutic synergism.
  • Methods of treating cancer can include administering to a subject a therapeutically effective amount of a compound or formulation described herein.
  • the compounds described herein can function as proteasome inhibitors.
  • Proteasome inhibitors induce apoptosis of cells by their ability to inhibit cellular proteasome activity. More specifically, in eukaryotic cells, the ubiquitin-proteasome pathway is the central pathway for protein degradation of intracellular proteins. Proteins are initially targeted for proteolysis by the attachment of a polyubiquitin chain, and then rapidly degraded to small peptides by the proteasome and the ubiquitin is released and recycled.
  • the 26S proteasome is a large (1,500-2,000 kDa) multi-subunit complex present in the nucleus and cytoplasm of eukaryotes.
  • the catalytic core of this complex referred to as the 20S proteasome, is a cylindrical structure consisting of four heptameric rings containing ⁇ - and ⁇ -subunits.
  • the proteasome is a threonine protease, the N-terminal threonine of the ⁇ -subunit providing the nucleophile that attacks the carbonyl group of the peptide bond in target proteins.
  • proteasome chymotryptic, tryptic and peptidylglutamyl.
  • the ability to recognize and bind polyubiquitinated substrates is conferred by 19S (PA700) subunits, which bind to each end of the 20S proteasome. These accessory subunits unfold substrates and feed them into the 20S catalytic complex, whilst removing the attached ubiquitin molecules.
  • PA700 19S
  • Both the assembly of the 26S proteasome and the degradation of protein substrates are ATP-dependent ( Almond, Leukemia 16:433 (2002 )).
  • the ubiquitin-proteasome system regulates many cellular processes by the coordinated and temporal degradation of proteins.
  • the proteasome acts as a regulator of cell growth and apoptosis and disruption of its activity has profound effects on the cell cycle.
  • defective apoptosis is involved in the pathogenesis of several diseases including certain cancers, such as B cell chronic lymphocytic leukemia, where there is an accumulation of quiescent tumor cells.
  • Proteasome inhibitors as a class of compounds in general act by inhibiting protein degradation by the proteasome.
  • the class includes peptide aldehydes, peptide vinyl sulfones, which act by binding to and directly inhibiting active sites within the 20S core of the proteasome. Peptide aldehydes and peptide vinyl sulfones, however, bind to the 20S core particle in an irreversible manner, such that proteolytic activity cannot be restored upon their removal.
  • peptide boronic acid compounds such as those described herein, confer stable inhibition of the proteasome, yet dissociate slowly from the proteasome.
  • the peptide boronic acid compounds are more potent than their peptide aldehyde analogs, and act more specifically in that the weak interaction between boron and sulfur means that peptide boronates do not inhibit thiol proteases ( Richardson, P. G., et al., Cancer Control. 10(5):361, (2003 )).
  • proteasome inhibitors Exposure of a variety of tumor-derived cell lines to proteasome inhibitors triggers apoptosis, likely as a result of effects on several pathways, including cell cycle regulatory proteins, p53, and nuclear factor kappa B (NF- ⁇ B) ( Grimm, L. M. and Osborne, B. A., Results Probl. Cell. Differ. 23:209-28 (1999 ); Orlowski, R. Z., Cell Death Differ. 6(4):303-13 (1999 )). Many of the initial studies documenting proteasome inhibitor-mediated apoptosis used cells of hematopoietic origin, including monoblasts ( Imajoh-Ohmi, S. et al., Biochem. Biophys. Res. Commun.
  • T-cell and lymphocytic leukemia cells Shinohara, K. et al., Biochem. J. 317(Pt 2):385-88, (1996 )
  • lymphoma cells Tanimoto, Y. et al., J. Biochem. (Tokyo) 121 (3):542-49 (1997 )
  • promyelocytic leukemia cells Drexler, H. C., Proc. Natl. Acad. Sci. U.S.A. 94(3):855-60 (1997 )).
  • the first demonstration of in vivo antitumor activity of a proteasome inhibitor used a human lymphoma xenograft model ( Orlowski, R.
  • proteasome inhibitors were reported to induce preferential apoptosis of patient-derived lymphoma ( Orlowski, R. et al. Cancer. Res.,58:(19):4342 (1998 )) and leukemia cells ( Mas favour, P. et al., Br. J. Haematol. 105(3):752-57 (1999 )) and to preferentially inhibit proliferation of multiple mycloma cells ( Hidcshima, T. et al., Cancer Res., 61(7): 3071-76 (2001 )) with relative sparing of control, non-transformed cells.
  • proteasome inhibitors are particularly useful as therapeutic agents in patients with refractory hematologic malignancies.
  • a compound or formulation described herein is used for treatment of cancer, and more particularly for treatment of a tumor in a cancer patient.
  • the cancer can be a tumor.
  • the cancer can also be stomach cancer, kidney cancer, bone cancer, liver cancer, brain cancer, skin cancer, oral cancer, lung cancer, pancreatic cancer, colon cancer, intestinal cancer, myeloid leukemia, melanoma, glioma, thyroid follicular cancer, bladder carcinoma, myelodysplastic syndrome, breast cancer, low grade astrocytoma, astrocytoma, glioblastoma, medulloblastoma, renal cancer, prostate cancer, endometrial cancer, or a neuroblastoma.
  • the cancer can be multiple myeloma.
  • Multiple myeloma is an incurable malignancy that is diagnosed in approximately 15,000 people in the United States each year ( Richardson, P. G. et al., Cancer Control. 10(5):361 (2003 )). It is a hematologic malignancy typically characterized by the accumulation of clonal plasma cells at multiple sites in the bone marrow. The majority of patients respond to initial treatment with chemotherapy and radiation; however, most eventually relapse due to the proliferation of resistant tumor cells.
  • provided are methods for treating multiple myeloma in a subject that can comprise administering a liposome formulation comprising a compound described herein.
  • the cancer can be breast cancer.
  • the compounds and formulations described herein can be effective in breast cancer treatment by helping to overcome some of the major pathways by which cancer cells resist the action of chemotherapy. For example, signaling through NF-kB, a regulator of apoptosis, and the p44/42 mitogen-activated protein kinase pathway, can be anti-apoptotic. Since proteasome inhibitors block these pathways, the compounds are able to activate apoptosis.
  • methods for treating breast cancer in a subject can comprise administering a liposome formulation comprising a compound described herein.
  • chemotherapeutic agents such as taxanes and anthracyclines have been shown to activate one or both of these pathways
  • use of a proteasome inhibitor in combination with conventional chemotherapeutic agents acts to enhance the antitumor activity of drugs, such as paclitaxel and doxorubicin.
  • a chemotherapeutic agent in free form or in liposome-entrapped form, is administered in combination with a compound or formulation described herein.
  • Doses and a dosing regimen for the compounds and formulations described herein will depend on the cancer being treated, the stage of the cancer, the size and health of the patient, and other factors readily apparent to an attending medical caregiver.
  • Clinical studies with the proteosome inhibitor bortezomib, Pyz-Phe-boroLeu (PS-341) can be used to provide guidance for selecting suitable dosages and dosing regimens. For example, given intravenously once or twice weekly, the maximum tolerated dose in patients with solid tumors was 1.3 mg/m 2 ( Orlowski, R. Z. et al., Breast Cancer Res. 5:1-7 (2003 )).
  • bortezomib given as an intravenous bolus on days 1, 4, 8, and 11 of a 3-week cycle suggested a maximum tolerated dose of 1.56 mg/m 2 ( Vorhees, P. M. et al., Clinical Cancer Res. 9:6316 (2003 )).
  • liposomal BTZ is less toxic than free BTZ, the optimal clinical dose of the liposomal drug can be several times higher.
  • the compounds and formulations described herein can be administered parenterally (e.g., by intravenous administration or subcutaneous administration). It will be appreciated that the formulation can include any necessary or desirable pharmaceutical excipients to facilitate delivery.
  • the compounds and formulation disclosed herein can also be administered via oral route, by i.p. injection, by intramuscular injection, intratumoral injection, and by airway administration as a micronized solid or liquid aerosol.
  • administration and variants thereof (e.g., “administering” a compound) in reference to a compound as described herein means introducing the compound or a formulation thereof into the system of a subject in need of treatment.
  • a compound as described herein or a formulation thereof is provided in combination with one or more other active agents (e.g., a cytotoxic agent, etc.)
  • “administration” and its variants are each understood to include concurrent and sequential introduction of the compound or formulation thereof and other agents.
  • the disclosed compounds can be formulated in a physiologically- or pharmaceutically-acceptable form and administered by any suitable route known in the art including, for example, oral, nasal, rectal, topical, and parenteral routes of administration.
  • parenteral includes subcutaneous, intradermal, intravenous, intramuscular, intraperitoneal, and intrasternal administration, such as by injection.
  • Administration of the disclosed compounds or formulations can be a single administration, or at continuous or distinct intervals as can be readily determined by a person skilled in the art.
  • the compounds disclosed herein, and formulations comprising them can also be administered utilizing liposome technology, slow release capsules, implantable pumps, and biodegradable containers. These delivery methods can, advantageously, provide a uniform dosage over an extended period of time.
  • the compounds can also be administered in their salt derivative forms or crystalline forms.
  • the compounds disclosed herein can be formulated according to known methods for preparing pharmaceutically acceptable compositions. Formulations are described in detail in a number of sources which are well known and readily available to those skilled in the art. For example, Remington's Pharmaceutical Science by E.W. Martin (1995 ) describes formulations that can be used in connection with the disclosed methods. In general, the compounds disclosed herein can be formulated such that an effective amount of the compound is combined with a suitable carrier in order to facilitate effective administration of the compound.
  • the formulations used can also be in a variety of forms. These include, for example, solid, semi-solid, and liquid dosage forms, such as tablets, pills, powders, liquid solutions or suspension, suppositories, injectable and infusible solutions, and sprays.
  • compositions disclosed herein can advantageously comprise between about 0.1% and 99%, and especially, 1 and 15% by weight of the total of one or more of the subject compounds based on the weight of the total formulation including carrier or diluent.
  • Formulations suitable for administration include, for example, aqueous sterile injection solutions, which can contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood of the intended recipient; and aqueous and nonaqueous sterile suspensions, which can include suspending agents and thickening agents.
  • the formulations can be presented in unit-dose or multi-dose containers, for example sealed ampoules and vials, and can be stored in a freeze dried (lyophilized) condition requiring only the condition of the sterile liquid carrier, for example, water for injections, prior to use.
  • Extemporaneous injection solutions and suspensions can be prepared from sterile powder, granules, tablets, etc. It should be understood that in addition to the ingredients particularly mentioned above, the compositions disclosed herein can include other agents conventional in the art having regard to the type of formulation in question.
  • the compounds disclosed herein can be administered to a patient in need of treatment in combination with other antitumor or anticancer substances and/or with radiation and/or photodynamic therapy and/or with surgical treatment to remove a tumor.
  • these other substances or treatments can be given at the same as or at different times from the compounds disclosed herein.
  • the compounds disclosed herein can be used in combination with mitotic inhibitors such as taxol or vinblastine, alkylating agents such as cyclophosamide or ifosfamide, antimetabolites such as 5-fluorouracil or hydroxyurea, DNA intercalators such as adriamycin or bleomycin, topoisomerase inhibitors such as etoposide or camptothecin, antiangiogenic agents such as angiostatin, antiestrogens such as tamoxifen, and/or other anti-cancer drugs or antibodies, such as, for example, GLEEVEC (Novartis Pharmaceuticals Corporation) and HERCEPTIN (Genentech, Inc.), respectively.
  • mitotic inhibitors such as taxol or vinblastine
  • alkylating agents such as cyclophosamide or ifosfamide
  • antimetabolites such as 5-fluorouracil or hydroxyurea
  • DNA intercalators such as adriamycin or bleomycin
  • Epstein-Barr Virus is associated with a number of mammalian malignancies.
  • the compounds disclosed herein can also be used alone or in combination with anticancer or antiviral agents, such as ganciclovir, azidothymidine (AZT), lamivudine (3TC), etc., to treat patients infected with a virus that can cause cellular transformation and/or to treat patients having a tumor or cancer that is associated with the presence of viral genome in the cells.
  • anticancer or antiviral agents such as ganciclovir, azidothymidine (AZT), lamivudine (3TC), etc.
  • the compounds can be used with mutant herpes simplex virus in the treatment of non-small cell lung cancer ( Toyoizumi, et al., "Combined therapy with chemotherapeutic agents and herpes simplex virus type IICP34.5 mutant (HSV-1716) in human non-small cell lung cancer," Human Gene Therapy, 1999, 10(18):17 ).
  • Compounds and formulations disclosed herein can be locally administered at one or more anatomical sites, such as sites of unwanted cell growth (such as a tumor site or benign skin growth, e.g., injected or topically applied to the tumor or skin growth), optionally in combination with a pharmaceutically acceptable carrier such as an inert diluent.
  • a pharmaceutically acceptable carrier such as an inert diluent
  • Compounds and formulations disclosed herein can be systemically administered, such as intravenously or orally, optionally in combination with a pharmaceutically acceptable carrier such as an inert diluent, or an assimilable edible carrier for oral delivery. They can be enclosed in hard or soft shell gelatin capsules, can be compressed into tablets, or can be incorporated directly with the food of the patient's diet.
  • the active compound can be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, aerosol sprays, and the like.
  • the tablets, troches, pills, capsules, and the like can also contain the following: binders such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, fructose, lactose or aspartame or a flavoring agent such as peppermint, oil of wintergreen, or cherry flavoring can be added.
  • a liquid carrier such as a vegetable oil or a polyethylene glycol.
  • any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed.
  • the active compound can be incorporated into sustained-release preparations and devices.
  • compositions disclosed herein can be administered intravenously, intramuscularly, or intraperitoneally by infusion or injection.
  • Solutions of the active agent or its salts can be prepared in water, optionally mixed with a nontoxic surfactant.
  • Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations can contain a preservative to prevent the growth of microorganisms.
  • the pharmaceutical dosage forms suitable for injection or infusion can include sterile aqueous solutions or dispersions or sterile powders comprising the active ingredient, which are adapted for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes.
  • the ultimate dosage form should be sterile, fluid, and stable under the conditions of manufacture and storage.
  • the liquid carrier or vehicle can be a solvent or liquid dispersion medium comprising, for example, water, ethanol, a polyol (for example, glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, nontoxic glyceryl esters, and suitable mixtures thereof.
  • the proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions or by the use of surfactants.
  • the prevention of the action of microorganisms can be brought about by various other antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars, buffers or sodium chloride.
  • Prolonged absorption of the injectable compositions can be brought about by the inclusion of agents that delay absorption, for example, aluminum monostearate and gelatin.
  • Sterile injectable solutions are prepared by incorporating a compound and/or agent disclosed herein in the required amount in the appropriate solvent with various other ingredients enumerated above, as required, followed by filter sterilization.
  • the preferred methods of preparation are vacuum drying and the freeze drying techniques, which yield a powder of the active ingredient plus any additional desired ingredient present in the previously sterile-filtered solutions.
  • compounds and agents disclosed herein can be applied in as a liquid or solid. However, it will generally be desirable to administer them topically to the skin as formulations, in combination with a dermatologically acceptable carrier, which can be a solid or a liquid.
  • a dermatologically acceptable carrier which can be a solid or a liquid.
  • Compounds and agents and formulations disclosed herein can be applied topically to a subject's skin to reduce the size (and can include complete removal) of malignant or benign growths, or to treat an infection site.
  • Compounds and agents disclosed herein can be applied directly to the growth or infection site.
  • the compounds and agents are applied to the growth or infection site in a formulation such as an ointment, cream, lotion, solution, tincture, or the like.
  • Drug delivery systems for delivery of pharmacological substances to dermal lesions can also be used, such as that described in U.S. Patent No. 5,167,649 .
  • Useful solid carriers include finely divided solids such as talc, clay, microcrystalline cellulose, silica, alumina and the like.
  • Useful liquid carriers include water, alcohols or glycols or water-alcohol/glycol blends, in which the compounds can be dissolved or dispersed at effective levels, optionally with the aid of non-toxic surfactants.
  • Adjuvants such as fragrances and additional antimicrobial agents can be added to optimize the properties for a given use.
  • the resultant liquid compositions can be applied from absorbent pads, used to impregnate bandages and other dressings, or sprayed onto the affected area using pump-type or aerosol sprayers, for example.
  • Thickeners such as synthetic polymers, fatty acids, fatty acid salts and esters, fatty alcohols, modified celluloses or modified mineral materials can also be employed with liquid carriers to form spreadable pastes, gels, ointments, soaps, and the like, for application directly to the skin of the user.
  • Examples of useful dermatological compositions which can be used to deliver a compound to the skin are disclosed in U.S. Patent No. 4,608,392 ; U.S. Patent No. 4,992,478 ; U.S. Patent No. 4,559,157 ; and U.S. Patent No. 4,820,508 .
  • Useful dosages of the compounds and agents and pharmaceutical formulations disclosed herein can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see U.S. Patent No. 4,938,949 .
  • compositions that comprise a compound disclosed herein in combination with a pharmaceutically acceptable carrier.
  • Pharmaceutical compositions adapted for oral, topical or parenteral administration, comprising an amount of a compound constitute a preferred aspect.
  • the dose administered to a patient, particularly a human should be sufficient to achieve a therapeutic response in the patient over a reasonable time frame, without lethal toxicity, and preferably causing no more than an acceptable level of side effects or morbidity.
  • dosage will depend upon a variety of factors including the condition (health) of the subject, the body weight of the subject, kind of concurrent treatment, if any, frequency of treatment, therapeutic ratio, as well as the severity and stage of the pathological condition.
  • compounds and agents and compositions disclosed herein can be administered to a patient in need of treatment prior to, subsequent to, or in combination with other antitumor or anticancer agents or substances (e.g., chemotherapeutic agents, immunotherapeutic agents, radiotherapeutic agents, cytotoxic agents, etc. ) and/or with radiation therapy and/or with surgical treatment to remove a tumor.
  • antitumor or anticancer agents or substances e.g., chemotherapeutic agents, immunotherapeutic agents, radiotherapeutic agents, cytotoxic agents, etc.
  • compounds and agents and compositions disclosed herein can be used in methods of treating cancer wherein the patient is to be treated or is or has been treated with mitotic inhibitors such as taxol or vinblastine, alkylating agents such as cyclophosamide or ifosfamide, antimetabolites such as 5-fluorouracil or hydroxyurea, DNA intercalators such as adriamycin or bleomycin, topoisomerase inhibitors such as etoposide or camptothecin, antiangiogenic agents such as angiostatin, antiestrogens such as tamoxifen, and/or other anti-cancer drugs or antibodies, such as, for example, GLEEVEC (Novartis Pharmaceuticals Corporation; East Hanover, NJ) and HERCEPTIN (Genentech, Inc.; South San Francisco, CA), respectively.
  • mitotic inhibitors such as taxol or vinblastine
  • alkylating agents such as cyclophosamide or ifosfamide
  • antimetabolites such as 5-flu
  • chemotherapeutic agents include, but are not limited to, altretamine, bleomycin, bortezomib (VELCADE), busulphan, calcium folinate, capecitabine, carboplatin, carmustine, chlorambucil, cisplatin, cladribine, crisantaspase, cyclophosphamide, cytarabine, dacarbazine, dactinomycin, daunorubicin, docetaxel, doxorubicin, epirubicin, etoposide, fludarabine, fluorouracil, gefitinib (IRESSA), gemcitabine, hydroxyurea, idarubicin, ifosfamide, imatinib (GLEEVEC), irinotecan, liposomal doxorubicin, lomustine, melphalan,
  • the chemotherapeutic agent is melphalan.
  • suitable immunotherapeutic agents include, but are not limited to, alemtuzumab, cetuximab (ERBITUX), gemtuzumab, iodine 131 tositumomab, rituximab, trastuzamab (HERCEPTIN).
  • Cytotoxic agents include, for example, radioactive isotopes (e.g., I 131 , I 125 , Y 90 , P 32 , etc.
  • toxins of bacterial, fungal, plant, or animal origin e.g., ricin, botulinum toxin, anthrax toxin, aflatoxin, jellyfish venoms ( e.g., box jellyfish, etc.
  • methods for treating an oncological disorder comprising administering an effective amount of a compound and/or agent disclosed herein prior to, subsequent to, and/or in combination with administration of a chemotherapeutic agent, an immunotherapeutic agent, a radiotherapeutic agent, or radiotherapy.
  • the disclosed subject matter also concerns a packaged dosage formulation comprising in one or more containers at least one inhibitor compound or composition disclosed herein, e.g., any compound of Formula I.
  • a packaged dosage formulation can optionally comprise in one or more containers a pharmaceutically acceptable carrier or diluent.
  • a suitable dose(s) can be that amount that will reduce proliferation or growth of the target cell(s).
  • a suitable dose(s) is that which will result in a concentration of the active agent in cancer tissue, such as a malignant tumor, which is known to achieve the desired response.
  • the preferred dosage is the amount which results in maximum inhibition of cancer cell growth, without unmanageable side effects.
  • Administration of a compound and/or agent can be continuous or at distinct intervals, as can be determined by a person of ordinary skill in the art.
  • compositions disclosed herein can comprise between about 0.1% and 45%, and especially, 1 and 15%, by weight of the total of one or more of the compounds based on the weight of the total composition including carrier or diluents.
  • dosage levels of the administered active ingredients can be: intravenous, 0.01 to about 20 mg/kg; intraperitoneal, 0.01 to about 100 mg/kg; subcutaneous, 0.01 to about 100 mg/kg; intramuscular, 0.01 to about 100 mg/kg; oral, 0.01 to about 100 mg/kg; of animal (body) weight.
  • the dosage levels of the administered active ingredients can be: intravenous, 0.01 to about 2.5 mg/kg; intraperitoneal, 0.01 to about 5 mg/kg; subcutaneous, 0.01 to about 5 mg/kg; intramuscular, 0.01 to about 5 mg/kg; oral, 0.01 to about 5 mg/kg; of animal (body) weight.
  • the dosage levels of the administered active ingredients can be: intravenous, 0.01 to about 1 mg/kg; intraperitoneal, 0.01 to about 5 mg/kg; subcutaneous, 0.01 to about 5 mg/kg; intramuscular, 0.01 to about 5 mg/kg; oral, 0.01 to about 5 mg/kg; of animal (body) weight.
  • the dosage levels of the administered active ingredients can be: intravenous, 0.01 to about 0.5 mg/kg; intraperitoneal, 0.01 to about 1 mg/kg; subcutaneous, 0.01 to about 1 mg/kg; intramuscular, 0.01 to about 1 mg/kg; oral, 0.01 to about 1 mg/kg; of animal (body) weight.
  • kits that comprise a composition comprising a compound disclosed herein in one or more containers.
  • the disclosed kits can optionally include pharmaceutically acceptable carriers and/or diluents.
  • a kit includes one or more other components, adjuncts, or adjuvants as described herein.
  • a kit includes one or more anti-cancer agents, such as those agents described herein.
  • a kit includes instructions or packaging materials that describe how to administer a compound or composition of the kit.
  • Containers of the kit can be of any suitable material, e.g., glass, plastic, metal, etc., and of any suitable size, shape, or configuration.
  • a compound and/or agent disclosed herein is provided in the kit as a solid, such as a tablet, pill, or powder form.
  • a compound and/or agent disclosed herein is provided in the kit as a liquid or solution.
  • the kit comprises an ampoule or syringe containing a compound and/or agent disclosed herein in liquid or solution form.
  • Meglumine was reacted with oleoyl chloride at a 1:1 molar ratio to yield N-methyl-N((4R,5R)-2,3,4,5,6-pentahydroxyhexyl)oleamide (OMG) (Scheme 1).
  • OMG was then coupled to BTZ to yield BTZ-OMG (Scheme 1).
  • L- ⁇ -phosphatidylcholine egg PC
  • cholesterol 1,2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE) conjugated polyethylene glycol (PEG) (mPEG-DSPE)
  • BTZ-OMG BTZ-OMG
  • Rotary evaporation was applied to form a dry lipid film, followed by hydration with calcium acetate buffer at a pH of 8.
  • Extrusion was used to reduce the liposome size to 150 nm or less. Any remaining unencapsulated drug was then removed through size exclusion chromatography on a Sepharose CL-4B column. Finally, the liposomes were sterile filtered and lyophilized.
  • the liposomes were made at pH 8, lyophilized in the presence of 10% sucrose as a lyoprotectant, and reconstituted shortly prior to use.
  • the liposome particle size distribution is determined through dynamic light scattering on a NTCOMP Submicron Particle Sizer Model 370.
  • the encapsulation efficiency was examined by a UV-visible spectrophotometer as the OD at 270 nm after 1:9 methanol extraction of fractions from the Sepharose CL-4B column ( Figure 1 ).
  • a reference measurement was also taken of the OD at 450 nm without methanol extraction ( Figure 1 ). Then, the ratio of total amount of drug content in the liposome fractions to total drug fractions was calculated. In this example, a drug entrapment of 41 % was obtained.
  • BTZ-OGA The synthetic methodology used to prepare BTZ-OGA is described in Scheme 2. Briefly, oleylglucamine (OGA) was synthesized from glucose, oleylamine and sodium cyanoborohydride using a Borch-type reductive amination. Then the OGA was coupled to BTZ, affording BTZ-OGA (Scheme 2). D-glucose and oleylamine at 1:1 molar ratio were co-dissolved and stirred in tert-butanol for 24 hr. Next, the mixture was cooled to 0°C in an ice bath and equal molar of NaCNBH 4 was added with continuously stirring until the evolution of hydrogen subsided. The mixture was acidified to a pH of 2-3 by the dropwise addition of concentrated HCl. The product precipitated in the form of HCl salt was isolated by centrifugation and washed with ice water.
  • OGA oleylglucamine
  • Egg L- ⁇ -phosphatidylcholine (egg PC), cholesterol, 1,2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE) conjugated polyethylene glycol (PEG) (mPEG-DSPE), and BTZ-OGA were dissolved in chloroform at a molar ratio of 40:36:4:20.
  • Rotary evaporation was applied to form a dry lipid film, followed by hydration with 50 mM sodium acetate buffer and 10% lactose at a pH of 8.5. Extrusion was used to reduce the liposome size to 150 nm or less. Any remaining unencapsulated drug was then removed through size exclusion chromatography on a Sepharose CL-4B column. Finally, the liposomes were sterile filtered and lyophilized.
  • the liposome particle size distribution was determined through dynamic light scattering on a NICOMP Submicron Particle Sizer Model 370.
  • the encapsulation efficiency was examined by a UV-visible spectrophotometer as the OD at 270 nm after 1:9 methanol dissolution of fractions collected from the Sepharose CL-4B column. A reference measurement was also taken of the OD at 450 nm without methanol dissolution. Then, the ratio of total amount of drug content in the liposome fractions to total drug fractions was calculated. In this example, the liposome particle size of 131.5 nm and a drug entrapment of 61 % were obtained.
  • a liposomal formulation based on MEGA-12 was also investigated.
  • Egg L- ⁇ -phosphatidylcholine (egg PC), cholesterol, 1,2-distearoyl-sn-glycero-3-phosphoethanolamine (DSPE) conjugated polyethylene glycol (PEG) (mPEG-DSPE), and BTZ-MEGA-12 were dissolved in chloroform at a molar ratio of 40:38:2:20.
  • Rotary evaporation was applied to form a dry lipid film, followed by hydration with 50 mM sodium acetate solution and 5 mM sodium phosphate buffer with 10% lactose at a pH of 8. Extrusion was used to reduce the liposome size to 150 nm or less. Any remaining unencapsulated drug was then removed through size exclusion chromatography on a Sepharose CL-4B column. Finally, the liposomes were sterile filtered and lyophilized.
  • the encapsulation efficiency of BTZ-MEGA-12 in the liposomal formulation was investigated by UV-vis, according to the methods described above. The results show that a drug entrapment of ⁇ 81.6% was obtained.
  • the liposome particle size distribution was determined through dynamic light scattering on a NICOMP Submicron Particle Sizer Model 370.
  • the encapsulation efficiency was examined by a UV-visible spectrophotometer as the OD at 270 nm after 1:9 methanol dissolution of fractions from the Sepharose CL-4B column. A reference measurement was also taken of the OD at 450 nm without methanol extraction. Then, the ratio of total amount of drug content in the liposome fractions to total drug fractions was calculated. In this example, the liposome particle size of 97.3 nm was obtained.
  • the product was analyzed by thin-layer chromatography and had an R f of 0.50 (methanol:chloroform, 1 :2, v/v).
  • the product was also analyzed by HPLC (using a Thermo Finnigan Surveyor HPLC system).
  • BTZ-MEGA-CHOL was prepared by combining BTZ with MEGA-CHOL in tert- butanol at room temperature, and lyophilizing the mixture.
  • 1 H NMR (CDCl 3 ): 0.68 (s, 6H, HC); 0.88-1.12 (m, 30H, -CH 3 ); 1.26-1.48 (s, 14H (alkyl BTZ)); 1.61 (m, 10 H, -CH 2 (side chain)); 1.84-2.43 (m, 10H, HC(ring)); 2.62 (s, 7H,meglumine H); 2.97 (s, 4H, CH2), 3.20 (s, 2H, BTZ benzene ring conjugated CH 2 ), 3.80-3.96 (m, 10 H, meglumine H); 4.45 (s, 1 H, H-C-C-O), 5.37 (s, 1H, , H-C C), 7.20 (m, 5H, benzene ring, overlapped by CHCl 3 solvent peak), 8.
  • BTZ-MEGA-CHOL was synthesized in chloroform using a 2x excess of MEGA-CHOL at room temperature, and incorporated into the liposomes in a continuous process.
  • BTZ and MEGA-CHOL at molar ratio of 1:2 were dissolved in chloroform and incubated overnight at room temperature.
  • the resulting complex BTZ-MEGA-CHOL
  • Rotary evaporation was used to form a dry lipid film in a round-bottom flask, followed by vacuum drying for another 2 hrs.
  • Buffer containing 50 mM sodium acetate and 10 mM glycine at pH 8 was used to hydrate this film at a lipid concentration of 50 mg/ml. Sonication was then applied to reduce particle size to 200 nm or smaller. Next, sample was loaded on a Sepharose CL-4B column to remove free BTZ. Fractions containing L-BTZ were collected and 10% sucrose was added. This product was then filtered through a 0.22 ⁇ m membrane filter and lyophilized.
  • the encapsulation efficiency of the drug was investigated by UV-vis, as described above. Specifically, the lyophilized prodrug BTZ-MEGA-CHOL was reconstituted in ddH 2 O and loaded on a Sepharose CL-4B column and the eluate was collected at 1 mL per fraction. Each fraction was analyzed by UV-vis spectrophotometry.
  • Figure 4 displays the normalized results for BTZ-MEGA-CHOL (e.g., Y-axis is the absorbance of each fraction after the substraction of the absorbance values of the control). A drug entrapment efficiency of 80.11% was obtained.
  • the colloidal stability of lyophilized liposomal formulations of BTZ-MEGA-CHOL was evaluated.
  • the lyophilized liposomal formulation of BTZ-MEGA-CHOL was stored at room temperature and monitored over time. At varying intervals over 28 weeks, the lyophilized liposomal formulation of BTZ-MEGA-CHOL was re-hydrated, and the particle size was measured as described above.
  • the results arc plotted in Figure 5 . The results shown are the mean of 3 separate experiments, and the error bars represent the standard deviation.
  • the lyophilized liposomal formulation of BTZ-MEGA-CHOL was also evaluated by cryo-transmission electron microscopy (Cryo-TEM).
  • Chro-TEM cryo-transmission electron microscopy
  • One drop of sample containing lyophilized liposomes including BTZ-MEGA-CHOL was added to each glow-discharged holey carbon/formvar film coated grid in a controlled environment vitrification system at constant humidity and temperature of 25°C.
  • the samples were blotted and vitrified by immediately plunging into a bath of liquid ethane slush.
  • mice were injected with 5 x 10 5 MV4-11 AML cells.
  • the mice were divided into two groups of 10 each (Trial I), and were treated with empty liposomes or the liposomal formulation of BTZ-MEGA-CHOL at 1 mg/kg, twice a week, by tail vein injection.
  • the study was repeated once with 5 mice in each group (Trial II). Three mice from each group were sacrificed after 4 weeks of treatment in Trial I for further analysis.
  • mice 6-8 week-old NSG mice (NOD.Cg-Prkdcscid H2rgtm1 Wj1/SzJ, The Jackson Laboratory, Bar Harbor, ME) were intravenously (i.v.) injected through tail vein with 0.3X 106 adapted MV4-11 cells. Both empty liposomes and L-BTZ were given for 4 weeks and then sacrificed. In the study, 3 mice per group were analyzed. Leukemic blast cells from peripheral blood of the mice from both of groups were analyzed by histological staining. In addition, the mice were evaluated spleen size and weight. The blood smear from both group were stained with Wright-Giemsa and the leukemic blast cells were visualized under the microscope. There was significant different in spleen size of L-BTZ treated group ( Figure 12 ). There were very few blast cells and the spleen was smaller compared with empty liposome treated group ( Figure 13 ).
  • the rate of BTZ release from BTZ prodrug was determined by monitoring the change in drug content in liposomes over time in pH 7.4 phosphate-buffered saline (PBS) at 37°C.
  • PBS pH 7.4 phosphate-buffered saline
  • L-BTZ (2ml) was diluted by 18 mL of PBS with continuous stirring at 37°C. At various time intervals, 1 mL of sample was removed for analysis. Separation of L-BTZ from free BTZ was done by loading 1 mL of L-BTZ mixture through a 10 mL Sepharose CL-4B column at 1 mL per fraction equilibrated by water. Each fraction was then extracted by 9x methanol.
  • the Pharmacokinetics of L-BTZ was studied in ICR mice (Charles River Lab, Wilmington, MA). The PK profile of free BTZ was also determined. Mice were given intravenous injections of free BTZ or L-BTZ at 1.0 mg/kg body weight via tail vein. At selected time intervals, a minimum of 100 ⁇ L blood plasma was collcctcd from each mouse using heparin-containing tubes. Plasma was then isolated by centrifugation at 3000x g for 5 min. The drug concentration in plasma was determined by measuring Boron concentration through an inductively coupled plasma-optical emission spectrometer (ICP-OES). The Boron extraction and sample preparation has been described previously. The plasma concentration vs. time plot was shown in Figure 15 .
  • ICP-OES inductively coupled plasma-optical emission spectrometer
  • L-BTZ was evaluated using a standard LAL assay. The results of the LAL assay are included in Table 2 below. Table 2. Results of LAL Assay. Sample LAL Assay, EU/mg BTZ (% Spike Recovery) Chromogenic Turbidity L-BTZ 1746 (102) 1060 (132) Endotoxin Limit 30.8 30.8
  • the zeta potential of the liposomes in the L-BTZ formulation was also measured.
  • a sample of L-BTZ was diluted 100 fold with 10 mM NaCl.
  • the apparent zeta potential was then measured at 25°C and a pH of 7.5.
  • the liposomes had a negative zeta potential value of -16.1 ⁇ 0.3 mV.
  • BTZ and MEGA-CHOL (molar ratio 1:2) were dissolved in isopropanol and reacted for two hours.
  • DSPC, cholesterol, and PEG-DSPE were then added into solution until they were completely dissolved.
  • the above L-BTZ suspension was processed on a high-pressure homogenizer (Avestin Emulsiflex C5) at 10,000 psi with continuous processing to reduce the mean particle size to below 100 nm. And then the L-BTZ was filtered through 0.45 ⁇ m filter to remove any insoluble particles before tangential flow diafiltration (TFF).
  • a high-pressure homogenizer Avestin Emulsiflex C5
  • the L-BTZ was filtered through 0.45 ⁇ m filter to remove any insoluble particles before tangential flow diafiltration (TFF).
  • TFF system Micropore Labscale TFF pump system used with a Midikros hollow fiber cartridge
  • sucrose cryoprotectant

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Claims (15)

  1. Verbindung, definiert durch Formel IA
    Figure imgb0036
     wobei
    Z zusammen mit O1 und O2 eine von Polyol abgeleitete Einheit darstellt, wobei das Polyol einen Zucker und 2 bis 8 Hydroxylgruppen umfasst;
    L fehlt oder eine Verknüpfungsgruppe ist, ausgewählt aus:
    einer Alkylengruppe, einer Heteroalkylengruppe, einer Alkenylengruppe, einer Heteroalkenylengruppe, einer Alkinylengruppe, einer Heteroalkinylengruppe, einer Cycloalkylengruppe, einer Alkylcycloalkylengruppe, einer Cycloalkylalkylengruppe, einer Heterocyclylengruppe, einer Alkylheterocyclylengruppe, einer Heterocyclylalkylengruppe, einer Alkylcarbonylgruppe, einer Alkoxycarbonylgruppe, einer Alkylaminocarbonylgruppe, einer Heteroalkylarninocarbonylgruppe, einer Dialkylarninocarbonylgruppe, einer Heterodialkylaminocarbonylgruppe, einer sekundären Amideinheit, einer tertiären Amideinheit, einer sekundären Carbamateinheit, einer tertiären Carbamateinheit, einer Harnstoffeinheit, einer Carbinoleinheit, einer Ethereinheit, einer Estereinheit, einer Imineinheit und einer Disulfidverknüpfung; und
    A eine Lipideinheit, ausgewählt aus einer Fettsäure, einem Glycerolipid, einem Phospholipid, einem Sphingolipid, einem Sterol oder einem Prenol, umfasst.
  2. Verbindung nach Anspruch 1, wobei das Polyol ein Monosaccharid umfasst.
  3. Verbindung nach Anspruch 1 oder Anspruch 2, wobei das Polyol einen reduzierten Zucker umfasst.
  4. Verbindung nach einem der vorhergehenden Ansprüche, wobei das Polyol einen Aminozucker umfasst.
  5. Verbindung nach einem der vorhergehenden Ansprüche, wobei es sich bei dem Polyol um Meglumin, Glucamin, Mannitol, Sorbitol oder Fructose handelt.
  6. Verbindung nach einem der vorhergehenden Ansprüche, wobei es sich bei A um eine C8-C40-Alkylgruppe, eine C8-C40-Alkenylgruppe, eine C8-C40-Alkoxygruppe, eine C8-C40-Alkylthiogruppe, eine C8-C40-Alkylsulfinylgruppe, eine C8-C40-Alkylsulfonylgruppe, eine C8-C40-Alkylaminogruppe, eine C8-C40-Dialkylaminogruppe, eine C8-C40-Alkylcarbonylgruppe, eine C8-C40-Alkoxycarbonylgruppe, eine C8-C40-Alkylaminocarbonylgruppe, eine C8-C40-Dialkylaminocarbonylgruppe oder eine durch die vorstehende Formel definierte Einheit handelt,
    Figure imgb0037
     wobei
    die gepunkteten Linien angeben, dass eine einfache Bindung oder eine Doppelbindung vorhanden sein kann;
    R6 eine Alkylgruppe, eine Alkenylgruppe, eine Alkinylgruppe, eine Arylgruppe, eine Alkylarylgruppe, eine Arylalkylgruppe, eine Cycloalkylgruppe, eine Alkylcycloalkylgruppe, eine Heterocyclylgruppe, eine Alkylheterocyclylgruppe, eine Heteroarylgruppe, eine Alkylheteroarylgruppe, eine Alkoxygruppe oder eine Alkylthiogruppe ist; und
    R7, R8, R9, R10 und R11 unabhängig Wasserstoff, eine Hydroxygruppe, eine Aminogruppe, eine Alkylgruppe, eine Alkenylgruppe, eine Alkinylgruppe, eine Arylgruppe, eine Alkylarylgruppe, eine Arylalkylgruppe, eine Cycloalkylgruppe, eine Alkylcycloalkylgruppe, eine Heterocyclylgruppe, eine Alkylheterocyclylgruppe, eine Heteroarylgruppe, eine Alkylheteroarylgruppe, eine Alkoxygruppe, eine Alkylthiogruppe, eine Alkylsulfinylgruppe, eine Alkylsulfonylgruppe, eine Alkylaminogruppe, eine Dialkylaminogruppe, eine Alkylcarbonylgruppe, eine Alkoxycarbonylgruppe, eine Alkylaminocarbonylgruppe oder eine Dialkylaminocarbonylgruppe sind.
  7. Verbindung nach einem der vorhergehenden Ansprüche, wobei die Verbindung definiert ist durch Formel IIA
    Figure imgb0038
     wobei
    X -O- oder -NR12- ist;
    R12 Wasserstoff oder eine Alkylgruppe ist,
    L fehlt oder eine Verknüpfungsgruppe ist; und
    A eine Lipid Einheit ist.
  8. Verbindung nach Anspruch 7, wobei X-NH- oder -N(CH3)- ist.
  9. Verbindung nach einem der vorhergehenden Ansprüche, wobei es sich bei der Verbindung um
    Figure imgb0039
    Figure imgb0040
    Figure imgb0041
    Figure imgb0042
     oder
    Figure imgb0043
     handelt.
  10. Pharmazeutische Formulierung, umfassend
    (i) aus einem Vesikel-bildenden Lipid gebildete Liposomen; und
    (ii) eine in den Liposomen eingeschlossene Verbindung nach einem der vorhergehenden Ansprüche.
  11. Pharmazeutische Formulierung nach Anspruch 10, wobei die Formulierung lyophilisiert ist.
  12. Formulierung nach Anspruch 10 oder Anspruch 11, wobei die Formulierung ferner ein Lyoprotektivum umfasst.
  13. Verbindung nach einem der Ansprüche 1 bis 9 oder Formulierung nach einem der Ansprüche 10 bis 12 zur Verwendung in einer Therapie.
  14. Verbindung nach einem der Ansprüche 1 bis 9 oder Formulierung nach einem der Ansprüche 10 bis 12 zur Verwendung in einem Verfahren zum Behandeln von Krebs.
  15. Lyophilisierte liposomale Formulierung, umfassend einen Boronsäureester von Bortezomib nach einem der Ansprüche 1 bis 9 zur Verwendung bei der Behandlung von Krebs durch orale Verabreichung.
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